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Despite CSM being known for nearly 100 years, many questions remain unanswered. Though our understanding of CSM is growing, it is still limited and the treatment of CSM remains controversial. is committed to supporting researchers answer these questions. If you have a research idea or project and would like support from, please get in touch. We are waiting to hear from you.

Alternatively, if you would simply like to share the highlights of a recent article or talk about what you are working on at the moment, we would be delighted to work with you to create a BLOG Post. Our community is always interested in keeping up to date with the research field.

Active Research Projects

If we can help support your research, please get in touch is currently supporting three international research projects:

Myelopathy Research -Code DCMThe first regenerative medicine trial for

Assessment Scales

a NIHR James Lind Alliance research priority setting
partnershiping partnership, to define the research questions that need answering.

RECODE-DCM is a consensus process to improve research efficiency in DCM, you can find more information about it here. : Our research in print

How Can You Get Involved?

When patient and the public are consulted in the design and delivery of research, its relevance and impact is higher! and its community is here to support your ‘PPI’ needs.

Get involved.

Health surveys are an important research tool. can help facilitate your research survey around the globe.

Share your CSM experience and help us solve the CSM mysteries!

Donate now, to help support future research projects.

What happens to my data in research? is committed to responsible research to advance our understanding of myelopathy, but these projects require your involvement to succeed. 

Research relies on individuals to share their experiences but, individuals are often nervous about sharing their personal information and uncertain how it is used. 

The following video has been produced by Connected Health Cities and The Farr Institute, who worked with patients and members of the public across the UK to understand the questions people have about patient data being used in research and produced a short film which explains how universities in the UK are using patient data to improve health and care, and the measures they must go to to ensure that your data remains safe and protected. is committed to responsible research and safe guarding our community. All supported projects must adhere to our code of conduct, have appropriate regulatory approval and be approved by our research committee. ​ adheres to the Health Research Authority policy for good practice in the management and conduct of health and social care research in the UK. If you have any further questions, queries or concerns about any of our research projects, please get in touch.